Suchergebnisse - "Giorgio Casari"

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giorgio casari » giorgio vasari (Erweiterte Suche)

1

Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2.

von: Loredana Leo

2011, in: PLoS Genetics

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2

Specific activation of GluN1-N2B NMDA receptors underlies facilitation of cortical spreading depression in a genetic mouse model of migraine with reduced astrocytic glutamate clearance

von: Giovanna Crivellaro

2021, in: Neurobiology of Disease

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3

Upregulation of Peroxiredoxin 3 Protects Afg3l2-KO Cortical Neurons In Vitro from Oxidative Stress: A Paradigm for Neuronal Cell Survival under Neurodegenerative Conditions

von: Barbara Bettegazzi

2019, in: Oxidative Medicine and Cellular Longevity

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4

Late onset motoneuron disorder caused by mitochondrial Hsp60 chaperone deficiency in mice

von: Raffaella Magnoni

2013, in: Neurobiology of Disease

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5

VarGenius-HZD Allows Accurate Detection of Rare Homozygous or Hemizygous Deletions in Targeted Sequencing Leveraging Breadth of Coverage

von: Francesco Musacchia

2021, in: Genes

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6

Retinal dystrophy in an individual carrying a de novo missense variant of SMARCA4

von: Gerarda Cappuccio

2019, in: Molecular Genetics & Genomic Medicine

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7

Cavitating and tigroid‐like leukoencephalopathy in a case of NDUFA2‐related disorder

von: Marianna Alagia

2020, in: JIMD Reports

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8

Novel

von: Michelle M. Monasky

2020, in: International Journal of Molecular Sciences

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9

Novel

von: Michelle M. Monasky

2021, in: International Journal of Molecular Sciences

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10

Impaired flickering of the permeability transition pore causes SPG7 spastic paraplegia

von: Irene Sambri

2020, in: EBioMedicine

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11

Mice harbouring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicity

von: Cecilia Mancini

2019, in: Neurobiology of Disease

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12

Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2

von: Mark A. Corbett

2019, in: Nature Communications

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13

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

von: Daniela Matuozzo

2023, in: Genome Medicine

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14

Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

von: Daniela Matuozzo

2024, in: Genome Medicine

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